Canonical Allele Identifier: CA5921631
Community Standard Title: NM_004211.5(SLC6A5):c.1948G>A (p.Val650Met)
Gene: SLC6A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.20638537G>A , CM000673.2:g.20638537G>A GRCh38
NC_000011.9:g.20660083G>A , CM000673.1:g.20660083G>A GRCh37
NC_000011.8:g.20616659G>A NCBI36
NG_013086.1:g.44138G>A
NG_013086.2:g.44138G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004211.5:c.1948G>A MANE Select NP_004202.4:p.Val650Met
ENST00000525748.6:c.1948G>A MANE Select ENSP00000434364.2:p.Val650Met
NM_001318369.1:c.1246G>A NP_001305298.1:p.Val416Met
NM_001318369.2:c.1246G>A NP_001305298.1:p.Val416Met
NM_004211.3:c.1948G>A NP_004202.2:p.Val650Met
NM_004211.4:c.1948G>A NP_004202.3:p.Val650Met
ENST00000298923.11:c.*1245G>A ENSP00000298923.7:n.*1245G>A
ENST00000525748.5:c.1948G>A ENSP00000434364.1:p.Val650Met
ENST00000528440.1:n.479G>A
XM_005253225.1:c.1246G>A XP_005253282.1:p.Val416Met
XM_011520473.1:c.1948G>A XP_011518775.1:p.Val650Met
XM_017018544.2:c.1072G>A XP_016874033.1:p.Val358Met
XM_017018545.2:c.907G>A XP_016874034.1:p.Val303Met